The Recall Desk

State

New Jersey product recalls

73,809 recalls have nationwide distribution and so reach New Jersey. 9,782 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total
9,782
Critical
1,246
Severe
2,944
Most recent
2026-11-04

Of the 9,782 recalls naming New Jersey we have scored against our rubric, 1,246 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,944 (30%) are Severe.

These figures cover only the 9,782 recalls whose distribution notice names New Jersey specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39076–39100 of 83591

  • ModerateFDA (Food)·F-1275-2019·2019-04-17

    Walgreens Probiotic Recalled for Incorrect Bacterial Strain

    Merical, LLC is recalling Walgreens Probiotic 12.5 Billion Active Cultures because the product contains a different bacterial strain than listed on the label.

    Product
    Walgreens Probiotic 12.5 Billion Active Cultures, 30 capsules; Dietary Supplement. Probiotic Blend 12.5 Billion CFU's L. rhamnosus HN001, L acidophilus La-14, L reuteri L.RE02. Other ingredients: Cellulose, Gelatin, Silicon Dioxide, Magnesium Stearate (vegetable…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1084-2019·2019-04-17

    X-Gen Recalls Clonidine Injection Vials Due to Labeling Error

    X-Gen Pharmaceuticals is recalling Clonidine HCL Injection vials because the side carton incorrectly lists the concentration as 500 mcg instead of 100 mcg per mL.

    Product
    CLONIDINE — CLONIDINE (CLONIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1082-2019·2019-04-17

    Auro Pharmacies Recalls Biotin Injection Vials for pH Failure

    Auro Pharmacies Inc. is recalling 167 vials of Biotin 10 mg/mL Injection because the product failed to meet its pH label claim.

    Product
    Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1134-2019·2019-04-17

    GE Healthcare Recalls Thallous Chloride TI 201 Injection Due to Chemical Contamination

    Medi-Physics Inc. dba GE Healthcare is recalling Thallous Chloride TI 201 Injection vials because trace amounts of an impurity were detected in the manufacturing reagent.

    Product
    Thallous Chloride TI 201 Injection, Specific Concentration: 37 MBq/mL (1 mCi/mL), Total Activity: 325.6 MBq (8.8 mCi) Volume: 8.8 mL vial, Rx Only, Mfg. by GE Healthcare, Medi-physics, Inc., Arlington Heights, IL 60004. NDC: 17156-299-18
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V306000·2019-04-16

    2019 Fleetwood and Holiday Rambler Motorhomes Recalled for Exhaust Defect

    REV is recalling 2019 Fleetwood Flair and Holiday Rambler Admiral motorhomes because the generator exhaust pipe placement may allow carbon monoxide to enter the vehicle.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER FLAIR, ADMIRAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E029000·2019-04-15

    Triumph Recalls Thruxton Motorcycles Due to Wiring Clearance Issue

    Triumph is recalling 2016-2018 Thruxton motorcycles because accessory fairing kits may damage wiring, causing loss of lights or engine stalls.

    Product
    TRIUMPH — TRIUMPH THRUXTON 1200R, THRUXTON 1200, THRUXTON A2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·19105·2019-04-12

    Fisher-Price Recalls Rock 'n Play Sleepers Due to Infant Death Reports

    Fisher-Price is recalling all Rock 'n Play Sleepers because over 30 infant fatalities have occurred. Consumers should stop using the product immediately and contact the company for a refund.

    Product
    All Models of Rock 'n Play Sleeper
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V298000·2019-04-12

    Honda and Acura Recall Vehicles Due to Timing Belt Defect

    Honda is recalling specific 2018-2019 Acura and Honda vehicles because timing belt teeth may separate, potentially causing an engine stall and increasing crash risk.

    Product
    HONDA — HONDA, ACURA PILOT, TLX, ODYSSEY, RIDGELINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V299000·2019-04-12

    Honda Recalls 2018-2019 Odyssey for Transmission Control Unit Reboot Risk

    Honda is recalling 2018-2019 Odyssey vehicles because loose battery connections may cause the transmission to shift to Park, potentially damaging the parking rod and increasing crash risk.

    Product
    HONDA — HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E028000·2019-04-12

    Cush Corp Recalls Trailer Axles Due to Wheel Separation Risk

    Cush Corp is recalling specific trailer suspension systems because a locking device may not be installed properly, allowing the wheel end to separate from the axle.

    Product
    SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V293000·2019-04-11

    Chrysler Recalls 2013-2016 Dodge Dart Vehicles for Shifter Cable Defect

    Chrysler is recalling 2013-2016 Dodge Dart vehicles with 6-speed automatic transmissions because the shifter cable bushing may fail, allowing the cable to detach and increasing crash risk.

    Product
    DODGE — DODGE DART
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V296000·2019-04-11

    Karma Revero Recall: Side Air Bags May Not Deploy in Rollover

    Karma Automotive is recalling 2018 Revero vehicles because side curtain air bags may not deploy in a rollover crash due to a disabled sensor system.

    Product
    KARMA — KARMA REVERO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V297000·2019-04-11

    Subaru Recalls Vehicles Due to Ignition Switch Spring Failure Risk

    Subaru is recalling specific 2005-2014 models because a broken spring in the ignition switch could cause the engine to turn off unexpectedly, increasing crash risk.

    Product
    SUBARU — SUBARU LEGACY, OUTBACK, IMPREZA, FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19103·2019-04-11

    DICK'S Recalls Field & Stream Tree Stands Due to Fall Hazard

    DICK'S Sporting Goods is recalling Field & Stream Timberline Hang On tree stands because the seat weld can break, posing a fall hazard.

    Product
    Field & Stream Timberline Hang On tree stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19104·2019-04-11

    Specialized Recalls Bicycles with Steerer Tube Collars Due to Fall Hazards

    Specialized is recalling about 63,000 bicycles because the steerer tube collar can crack, causing sudden loss of steering control and posing fall and injury hazards.

    Product
    Specialized Roubaix, Ruby, Diverge, and Sirrus Bicycles with steerer tube collars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V290000·2019-04-10

    Mercedes-Benz Metris Recalled for Corroding Power Steering Bolts

    Daimler Vans USA is recalling 2016-2017 Metris vans in 24 states and DC because aluminum power steering bolts may corrode and fracture, causing loss of steering assist.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V291000·2019-04-10

    BMW Recalls 2019 X3 and X4 Models Due to Air Bag Defect

    BMW is recalling 2019 X3 and X4 vehicles because the instrument panel may be improperly manufactured, potentially preventing the passenger air bag from deploying.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1235-2019·2019-04-10

    Better Made Potato Chips Recalled for Undeclared Milk

    Better Made Snack Foods is recalling 660 bags of Original Potato Chips due to undeclared milk. The product was sold in Michigan, Ohio, and via mail order nationwide.

    Product
    Better Made Snack Foods Family Size $3.99 Original Potato Chips 10oz. flexible pouch bag UPC code of 041633063048 12 bags per case
    Category
    Food
    Distribution
    Distributed nationwide